US2004242497A1PendingUtilityA1

Composition comprising paroxetine and a pharmaceutically acceptable glycyrrhizinate salt

Priority: Aug 9, 2001Filed: Aug 9, 2002Published: Dec 2, 2004
Est. expiryAug 9, 2021(expired)· nominal 20-yr term from priority
A61P 43/00A61K 9/0056A61K 9/2018A61P 25/22A61P 25/24A61K 47/26
14
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Claims

Abstract

A taste-masked formulation of paroxetine comprises a dry blend of paroxetine and a glycyrrhyzinate, especially paroxetine hydrochloride and ammonium glycyrrhyzinate, as a dispersible powder or moulded into a dispersible or chewable tablet.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A composition which is a dry blend of: 
 paroxetine free base, or a pharmaceutically acceptable salt or solvate of paroxetine, and a pharmaceutically acceptable glycyrrhyzinate salt.    
     
     
         2 . A pharmaceutical composition which is a dry blend of: 
 paroxetine free base, or a pharmaceutically acceptable salt or solvate of paroxetine, a pharmaceutically acceptable glycyrrhyzinate salt, and one or more pharmaceutically acceptable excipients.    
     
     
         3 . A composition according to  claim 2  which is in powder form.  
     
     
         4 . A composition according to  claim 2  which is a shaped composition.  
     
     
         5 . A composition according to  claim 2 , including one or more dispersing agents.  
     
     
         6 . A composition according to  claim 5  in which the dispersing agent is selected from polyvinyl pyrrolidone, calcium carbonate and sodium starch glycolate.  
     
     
         7 . A composition according to  claim 2  including one or more taste masking agents, sweeteners or flavourings.  
     
     
         8 . A composition according to  claim 1  in which the paroxetine salt is paroxetine hydrochloride.  
     
     
         9 . A composition according to  claim 1  in which the glycyrrhyzinate salt is ammonium glycyrrhyzinate.  
     
     
         10 . (Cancelled)  
     
     
         11 . Method of treating one or more of the Disorders which comprises administering a composition according to  claim 1  to a person suffering from one or more of the Disorders.

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